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rs1064793851

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CTCA;CTCA) 0 common in clinvar
Chromosome16
Position29813658
GenePRRT2
is asnp
is mentioned by
dbSNPrs1064793851
dbSNP (old)rs1064793851
ClinGenrs1064793851
ebirs1064793851
HLIrs1064793851
Exacrs1064793851
Gnomadrs1064793851
Varsomers1064793851
Maprs1064793851
PheGenIrs1064793851
Biobankrs1064793851
1000 genomesrs1064793851
hgdprs1064793851
ensemblrs1064793851
gopubmedrs1064793851
geneviewrs1064793851
scholarrs1064793851
googlers1064793851
pharmgkbrs1064793851
gwascentralrs1064793851
openSNPrs1064793851
23andMers1064793851
23andMe allrs1064793851
SNPshotrs1064793851
SNPdbers1064793851
MSV3drs1064793851
GWAS Ctlgrs1064793851
Max Magnitude0
ClinVar
Risk rs1064793851(-;-)
Alt rs1064793851(-;-)
Reference Rs1064793851(CTCA;CTCA)
Significance Pathogenic
Disease not provided
Variation info
Gene PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29824979_29824982delTCAC
CLNSRC
CLNACC RCV000485009.1,